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FDA Accepts Dupixent for Priority Review in Patients Aged 12 Years and Older with Eosinophilic Esophagitis

Regeneron Pharmaceuticals, Inc. and Sanofi announced the U.S. Food and Drug Administration (FDA) has accepted for Priority Review the supplemental Biologics License Application (sBLA)...

U.S. FDA Grants Priority Review to Genentech’s Actemra for the Treatment of COVID-19 in Hospitalized Adults

Genentech, a member of the Roche Group, announced that the U.S. Food and Drug Administration (FDA) has accepted the company’s supplemental Biologics License Application...

Mavacamten Demonstrated Significant Reduction in Need for Septal Reduction Therapy in Symptomatic Obstructive HCM Patients in Phase 3 VALOR Trial

Bristol Myers Squibb announced results from the Phase 3 VALOR-HCM study, which showed the addition of mavacamten, an investigational, first-in-class cardiac myosin inhibitor, significantly...

Cenobamate (ONTOZRY®), for the Treatment of Drug-Resistant Focal-Onset Seizures in Adults, Is Now Available in the Netherlands

Angelini Pharma, international pharmaceutical company part of the privately held Italian Angelini Group announced  that ONTOZRY® (cenobamate) is now available in the Netherlands for...

DISYS Partners with ComplianceQuest to Reduce Costs, Improve Safety and Sustainability in the Oil and Gas Industry

Global technology firm Digital Intelligence Systems, LLC (DISYS)  announced a partnership with ComplianceQuest, the leading provider of 100% cloud-native, AI-powered, Enterprise Clinical, Quality Health,...
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